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C101206

Sigma-Aldrich

1,4-Cyclohexanediol

99%

Synonym(s):

Hexahydrohydroquinone

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About This Item

Linear Formula:
C6H10(OH)2
CAS Number:
Molecular Weight:
116.16
Beilstein/REAXYS Number:
2036658
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

99%

form

powder

bp

150 °C/20 mmHg (lit.)

mp

98-100 °C (lit.)

SMILES string

OC1CCC(O)CC1

InChI

1S/C6H12O2/c7-5-1-2-6(8)4-3-5/h5-8H,1-4H2

InChI key

VKONPUDBRVKQLM-UHFFFAOYSA-N

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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

149.0 °F - closed cup

flash_point_c

65 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)


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Jun Wu et al.
Applied microbiology and biotechnology, 73(5), 1097-1105 (2006-09-16)
Commercial formulations of hexachlorocyclohexane (HCH) consist of a mixture of four isomers: alpha, beta, gamma, and delta. All four isomers are toxic and recalcitrant pollutants. beta-HCH is more problematic due to its longer persistence in the environment. Sphingomonas sp. BHC-A
Shuai Shuai Wu et al.
Cryo letters, 34(5), 497-507 (2014-01-23)
In this study, the fibroblasts cell line derived from ear marginal tissue of Yunnan semi-fine wool sheep was successfully established using the primary explants technique and cryopreservation technology. Additionally, the protective effect of synthetic ice blocker (SIB) including 1, 3-cyclohexanediol
G Giavaresi et al.
The International journal of artificial organs, 27(9), 796-805 (2004-11-04)
Two natural Biopol polyesters, containing 8% (D400G) and 12% (D600G) of hydroxyvalerate component, and a synthetic polyester based on 1,4 cyclohexanediol [Poly(cyclohexyl-sebacate)--PCS] were studied to investigate their in vitro and in vivo behavior for application in musculoskeletal tissue repair. The
James H Loehlin et al.
Acta crystallographica. Section B, Structural science, 64(Pt 5), 583-588 (2008-09-19)
The structure of a co-crystal with both trans and cis isomers of 1,4-cyclohexanediol (1,4-CHD) is reported. The intermolecular hydrogen-bond patterns are described and compared with those of the all trans structure, using the graph-set model. A second crystal with possible
Nan Li et al.
International journal of pharmaceutics, 387(1-2), 167-171 (2009-12-23)
The objective of this study is to investigate the effect of 1,4-cyclohexanediol as a retardant on the percutaneous absorption and penetration of azelaic acid. Hairless rat skin was mounted on Franz diffusion cells and treated with topical formulations containing solubilized

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